Variant #0000604771 (NC_000001.10:g.1469302C>G, ATAD3A(NM_018188.3):c.1759-4C>G)

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.1469302C>G
DNA change (hg38) g.1533922C>G
Published as ATAD3A(NM_018188.4):c.1759-4C>G
ISCN -
DB-ID ATAD3A_000042
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM240 NM_001114748.1 ?/. - c.*1437G>C r.(=) p.(=)
ATAD3A NM_018188.3 ?/. - c.1759-4C>G r.spl? p.?